Methionine restriction decreases visceral fat mass and preserves insulin action in aging male Fischer 344 rats independent of energy restriction

Summary Reduced dietary methionine intake (0.17% methionine, MR) and calorie restriction (CR) prolong lifespan in male Fischer 344 rats. Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of...

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Veröffentlicht in:Aging cell 2006-08, Vol.5 (4), p.305-314
Hauptverfasser: Malloy, Virginia L., Krajcik, Rozlyn A., Bailey, Steven J., Hristopoulos, George, Plummer, Jason D., Orentreich, Norman
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container_end_page 314
container_issue 4
container_start_page 305
container_title Aging cell
container_volume 5
creator Malloy, Virginia L.
Krajcik, Rozlyn A.
Bailey, Steven J.
Hristopoulos, George
Plummer, Jason D.
Orentreich, Norman
description Summary Reduced dietary methionine intake (0.17% methionine, MR) and calorie restriction (CR) prolong lifespan in male Fischer 344 rats. Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of insulin responsiveness in older animals. These studies examine the relationship between insulin responsiveness and visceral fat in MR and test whether, despite lower food intake observed in MR animals, decreased visceral fat accretion and preservation of insulin sensitivity is not secondary to CR. Accordingly, rats pair fed (pf) control diet (0.86% methinone, CF) to match the food intake of MR for 80 weeks exhibit insulin, glucose, and leptin levels similar to control‐fed animals and comparable amounts of visceral fat. Conversely, MR rats show significantly reduced visceral fat compared to CF and PF with concomitant decreases in basal insulin, glucose, and leptin, and increased adiponectin and triiodothyronine. Daily energy expenditure in MR animals significantly exceeds that of both PF and CF. In a separate cohort, insulin responses of older MR animals as measured by oral glucose challenge are similar to young animals. Longitudinal assessments of MR and CF through 112 weeks of age reveal that MR prevents age‐associated increases in serum lipids. By 16 weeks, MR animals show a 40% reduction in insulin‐like growth factor‐1 (IGF‐1) that is sustained throughout life; CF IGF‐1 levels decline much later, beginning at 112 weeks. Collectively, the results indicate that MR reduces visceral fat and preserves insulin activity in aging rats independent of energy restriction.
doi_str_mv 10.1111/j.1474-9726.2006.00220.x
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Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of insulin responsiveness in older animals. These studies examine the relationship between insulin responsiveness and visceral fat in MR and test whether, despite lower food intake observed in MR animals, decreased visceral fat accretion and preservation of insulin sensitivity is not secondary to CR. Accordingly, rats pair fed (pf) control diet (0.86% methinone, CF) to match the food intake of MR for 80 weeks exhibit insulin, glucose, and leptin levels similar to control‐fed animals and comparable amounts of visceral fat. Conversely, MR rats show significantly reduced visceral fat compared to CF and PF with concomitant decreases in basal insulin, glucose, and leptin, and increased adiponectin and triiodothyronine. Daily energy expenditure in MR animals significantly exceeds that of both PF and CF. In a separate cohort, insulin responses of older MR animals as measured by oral glucose challenge are similar to young animals. Longitudinal assessments of MR and CF through 112 weeks of age reveal that MR prevents age‐associated increases in serum lipids. By 16 weeks, MR animals show a 40% reduction in insulin‐like growth factor‐1 (IGF‐1) that is sustained throughout life; CF IGF‐1 levels decline much later, beginning at 112 weeks. 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Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of insulin responsiveness in older animals. These studies examine the relationship between insulin responsiveness and visceral fat in MR and test whether, despite lower food intake observed in MR animals, decreased visceral fat accretion and preservation of insulin sensitivity is not secondary to CR. Accordingly, rats pair fed (pf) control diet (0.86% methinone, CF) to match the food intake of MR for 80 weeks exhibit insulin, glucose, and leptin levels similar to control‐fed animals and comparable amounts of visceral fat. Conversely, MR rats show significantly reduced visceral fat compared to CF and PF with concomitant decreases in basal insulin, glucose, and leptin, and increased adiponectin and triiodothyronine. Daily energy expenditure in MR animals significantly exceeds that of both PF and CF. In a separate cohort, insulin responses of older MR animals as measured by oral glucose challenge are similar to young animals. Longitudinal assessments of MR and CF through 112 weeks of age reveal that MR prevents age‐associated increases in serum lipids. By 16 weeks, MR animals show a 40% reduction in insulin‐like growth factor‐1 (IGF‐1) that is sustained throughout life; CF IGF‐1 levels decline much later, beginning at 112 weeks. Collectively, the results indicate that MR reduces visceral fat and preserves insulin activity in aging rats independent of energy restriction.</description><subject>adipose</subject><subject>Adipose Tissue - drug effects</subject><subject>Adiposity</subject><subject>Aging</subject><subject>Animals</subject><subject>Body Composition - drug effects</subject><subject>Body Weight - drug effects</subject><subject>Cholesterol - metabolism</subject><subject>energy expenditure</subject><subject>Energy Intake</subject><subject>Energy Metabolism - drug effects</subject><subject>Glucose Tolerance Test</subject><subject>insulin</subject><subject>Insulin - blood</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Male</subject><subject>Methionine - deficiency</subject><subject>methionine restriction</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Time Factors</subject><subject>Triglycerides - metabolism</subject><issn>1474-9718</issn><issn>1474-9726</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctOwzAQRS0E4v0LyCt2DX7FdRYsqoqXVMQG1pbjTFpXqVPstNC_4JNxaFVY4oV9rTl3RjODEKYko-nczDMqhmJQDJnMGCEyI4Qxkn0eoNN94HCvqTpBZzHOCaHDgvBjdEKlIkQJeYq-nqGbudY7DzhA7IKzXfriCmwAEyHitYsWgmlwbTq8MDFi4yu8TDCEdYo7H1eN89hsjb2aOj9NaAP4PplnEDAXAgfT9XQFS0iX73BbY_AQppu_lS_QUW2aCJe79xy93d-9jh8Hk5eHp_FoMrBCcTIQUNcsNyWrcyaFsjZnQLnkpckLWlScqqKsCFdSMmsFlKVhucoLkSueXMLyc3S9zbsM7fsq1deLvtGmMR7aVdRSDSWhRCZQbUEb2hgD1HoZ3MKEjaZE99vQc90PWvdD1_029M829GeyXu1qrMoFVL_G3fgTcLsFPlwDm38n1qPx3SQp_g1nHpsw</recordid><startdate>200608</startdate><enddate>200608</enddate><creator>Malloy, Virginia L.</creator><creator>Krajcik, Rozlyn A.</creator><creator>Bailey, Steven J.</creator><creator>Hristopoulos, George</creator><creator>Plummer, Jason D.</creator><creator>Orentreich, Norman</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200608</creationdate><title>Methionine restriction decreases visceral fat mass and preserves insulin action in aging male Fischer 344 rats independent of energy restriction</title><author>Malloy, Virginia L. ; 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Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of insulin responsiveness in older animals. These studies examine the relationship between insulin responsiveness and visceral fat in MR and test whether, despite lower food intake observed in MR animals, decreased visceral fat accretion and preservation of insulin sensitivity is not secondary to CR. Accordingly, rats pair fed (pf) control diet (0.86% methinone, CF) to match the food intake of MR for 80 weeks exhibit insulin, glucose, and leptin levels similar to control‐fed animals and comparable amounts of visceral fat. Conversely, MR rats show significantly reduced visceral fat compared to CF and PF with concomitant decreases in basal insulin, glucose, and leptin, and increased adiponectin and triiodothyronine. Daily energy expenditure in MR animals significantly exceeds that of both PF and CF. In a separate cohort, insulin responses of older MR animals as measured by oral glucose challenge are similar to young animals. Longitudinal assessments of MR and CF through 112 weeks of age reveal that MR prevents age‐associated increases in serum lipids. By 16 weeks, MR animals show a 40% reduction in insulin‐like growth factor‐1 (IGF‐1) that is sustained throughout life; CF IGF‐1 levels decline much later, beginning at 112 weeks. Collectively, the results indicate that MR reduces visceral fat and preserves insulin activity in aging rats independent of energy restriction.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>16800846</pmid><doi>10.1111/j.1474-9726.2006.00220.x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source Wiley Online Library (Open Access Collection)
subjects adipose
Adipose Tissue - drug effects
Adiposity
Aging
Animals
Body Composition - drug effects
Body Weight - drug effects
Cholesterol - metabolism
energy expenditure
Energy Intake
Energy Metabolism - drug effects
Glucose Tolerance Test
insulin
Insulin - blood
Insulin-Like Growth Factor I - metabolism
Male
Methionine - deficiency
methionine restriction
Rats
Rats, Inbred F344
Time Factors
Triglycerides - metabolism
title Methionine restriction decreases visceral fat mass and preserves insulin action in aging male Fischer 344 rats independent of energy restriction
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